GapMind for Amino acid biosynthesis

 

Alignments for a candidate for cimA in Desulfovibrio vulgaris Miyazaki F

Align Putative (R)-citramalate synthase CimA; EC 2.3.3.21 (uncharacterized)
to candidate 8501897 DvMF_2612 pyruvate carboxyltransferase (RefSeq)

Query= curated2:A3CUF2
         (503 letters)



>FitnessBrowser__Miya:8501897
          Length = 455

 Score =  193 bits (491), Expect = 9e-54
 Identities = 140/378 (37%), Positives = 192/378 (50%), Gaps = 29/378 (7%)

Query: 13  DTTLRDGEQTPGVSLTPAGKLEIATHLADVGVHVIEAGSAAAS-VGERESIRAIADAGLA 71
           DTTLR+GEQ+ G  L+ A +  +   LA VGV   E G A    + +  ++ A    GLA
Sbjct: 4   DTTLREGEQSFGTYLSMADRERVLRGLAAVGVPEAEVGWAGREDLTDMLALSARVAPGLA 63

Query: 72  AECCTYVRALPGDIDLAADAGADSVHLVVPVSDLHIAKKLRKTREQVSEMAWSAVEYAKE 131
           A    + R  PGD+  A   GA  V + VPVSD H+A++L   R  + ++  + +  A+ 
Sbjct: 64  A--AAWCRCRPGDLRAAVACGASRVCVGVPVSDAHLARRLGLGRAALLDLLAATLAEARM 121

Query: 132 RGLV-VELSGEDASRADQDFLAEVFREGVERGADRLCFCDTVGLLTPERAAAII------ 184
            G+  V +  EDASRAD+ F+  V       GA R+   DTVGL TP   A ++      
Sbjct: 122 LGIEHVTVGMEDASRADRAFVFAVACHAAAHGAHRVRLSDTVGLYTPLEVADVVRALRAE 181

Query: 185 ----------PPLLFAPLSIHCHDDLGFGLATTVAALRAGATCAHVTVNGLGERAGNTSL 234
                     P      +  H H+D G   A  + AL  GA CA V+V GLGERAG   L
Sbjct: 182 LEGARQDDTAPRARRVSIGTHFHNDCGMATANALTALECGADCADVSVLGLGERAGVARL 241

Query: 235 EELVMALEVLYGVDTGIATEELYPLST---HVARLTGVPLATNKPIVGEMAFTHESGIHA 291
           EEL  AL V      G A  EL PL      VA+   + +  + P+ G   F  ESG+HA
Sbjct: 242 EELAAALVV-----RGRARFELAPLRALCGQVAQAASLSVPRHWPVAGRDIFAVESGLHA 296

Query: 292 HGVMRDASTYEPLQPERVGRRRRIVLGKHSGSAAVEAALHDMGYAPSAAQLKEIVDRIKR 351
           HGV RD S +EP  PE VG  RR+ +G+ SG AAV AAL ++   P   +L  IV+ ++ 
Sbjct: 297 HGVRRDPSLFEPFPPELVGDSRRMGVGRKSGVAAVAAALAELSILPPPDELPAIVEAVRD 356

Query: 352 LGDAGMR-ITDADIMAIA 368
           L     R +T A++  +A
Sbjct: 357 LSATLRRPLTPAELAEVA 374


Lambda     K      H
   0.318    0.134    0.376 

Gapped
Lambda     K      H
   0.267   0.0410    0.140 


Matrix: BLOSUM62
Gap Penalties: Existence: 11, Extension: 1
Number of Sequences: 1
Number of Hits to DB: 579
Number of extensions: 38
Number of successful extensions: 5
Number of sequences better than 1.0e-02: 1
Number of HSP's gapped: 1
Number of HSP's successfully gapped: 1
Length of query: 503
Length of database: 455
Length adjustment: 34
Effective length of query: 469
Effective length of database: 421
Effective search space:   197449
Effective search space used:   197449
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 51 (24.3 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory